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Label Proofreading Jobs (NOW HIRING)

krg technology inc

Proof Reader

Lake Forest, IL

... labeling artwork as well as a wide variety of other documentation, such as specifications ... artists with the proofreading of drawing templates (a visual diagram of a die drawing) for ...

Jobsbridge

Graphic Designer

San Diego, CA

... proofreading, and creating layout for product labels, and a variety of printed collateral Creating AI Photoshop/Illustrator compositions, editing and color correcting images Filing, faxing, emailing ...

Cesna Group

Package Design Associate

Rancho Cucamonga, CA · On-site

$50K - $100K/yr

Strong understanding of FDA labeling, Nutrition Facts formatting, and print production processes including dielines and prepress. * Excellent attention to detail, file organization, and proofreading ...

Omni Inclusive

Senior Proofreader

Princeton, NJ · On-site

... interacting with Labeling regarding issues that may arise • Have a working knowledge of ... years proofreading experience preferably in the pharmaceutical field • Strong written ...

Adept HR

Be Seen First

Customer Service Representative

Redlands, CA · On-site

$37K - $41K/yr

Generate UCC and Shipping Labels * Submit and collect routing requests * Create Bill of Ladings ... Handle administrative tasks such as filing, proofreading documents, and maintaining accurate ...

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Label Proofreading information

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How much do label proofreading jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for label proofreading in the United States is $27.65, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $33.65 per hour, depending on experience, location, and employer.

What is label proofreading?

Label proofreading is the process of reviewing and verifying product labels to ensure accuracy, compliance, and consistency with regulatory requirements and brand standards. This job involves checking for spelling and grammatical errors, verifying ingredient lists, ensuring legal information is correctly displayed, and confirming that all required elements are present. Label proofreaders often work closely with regulatory, design, and marketing teams to make sure labels meet industry standards and avoid costly mistakes before products go to market.

What is the difference between Label Proofreading vs Label Editing?

AspectLabel ProofreadingLabel Editing
FocusCorrecting spelling, grammar, and punctuation errorsImproving clarity, style, and consistency
Skills NeededAttention to detail, language proficiencyLanguage skills, editing expertise
Work EnvironmentLabel review, quality controlContent revision, document improvement
CertificationsNone required, but language certifications helpfulEditing certifications beneficial

Label Proofreading primarily involves checking labels for errors, ensuring accuracy and correctness. Label Editing goes a step further by refining the content for clarity and consistency. Both roles require strong language skills, but proofreading focuses on error correction, while editing emphasizes content improvement.

What are the key skills and qualifications needed to thrive as a Label Proofreader, and why are they important?

To thrive as a Label Proofreader, you need exceptional attention to detail, a strong command of language and grammar, and familiarity with regulatory requirements, often supported by a background in quality assurance or a related field. Proficiency with proofreading tools, document management systems, and specialized labeling software is typically required. Strong organizational skills, time management, and effective communication help you collaborate with cross-functional teams and meet tight deadlines. These skills are crucial to ensure label accuracy, regulatory compliance, and brand integrity in highly regulated industries.

What are some common challenges faced by label proofreaders, and how can they be addressed?

Label proofreaders often encounter challenges such as tight deadlines, complex regulatory requirements, and the need for extreme attention to detail, especially when working with multilingual or technical content. To address these challenges, it's important to develop strong organizational skills, stay updated on industry regulations, and use checklists or specialized proofreading tools to catch errors efficiently. Collaborating closely with regulatory, design, and production teams also helps ensure accuracy and clarity in the final product.
What cities are hiring for Label Proofreading jobs? Cities with the most Label Proofreading job openings:
What states have the most Label Proofreading jobs? States with the most job openings for Label Proofreading jobs include:
What job categories do people searching Label Proofreading jobs look for? The top searched job categories for Label Proofreading jobs are:
Label Proofreading jobs near you
Director, Regulatory Affairs (Labeling)

Director, Regulatory Affairs (Labeling)

Arrowhead Pharmaceuticals

Pasadena, CA • On-site

$163K - $216K/yr

Full-time

Posted 17 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
The Director of Regulatory Affairs is Arrowhead's Labeling lead, who drives cross-functional development and execution of global regulatory labeling strategy. This individual will manage regulatory labeling through all phases of development and post-approval (end-to-end) ensuring that the latest requirements and standards are met.
The ideal candidate will have experience collaborating with product and clinical development, medical, market access, and commercial stakeholders to generate phase and time-appropriate target product profile and labeling drafts, has successfully negotiated with health authorities, and global regulatory experience.
Responsibilities
  • Collaborate cross-functionally to develop labeling strategy and lead cross-functional Labeling meetings.
  • Manage development, review, approval, and version control of labeling documents, including Target Product Labeling, Core Labeling (e.g., Company Core Data Sheet [CCDS]), and Regional Labeling (e.g., USPI, EU SmPC), in a timely manner according to internal SOPs and external regulatory requirements.
  • Maintain expertise regarding key labeling requirements and stay current with labeling guidelines/regulations as they pertain to the development/maintenance of labeling and advise key stakeholders on the application of these labeling principles.
  • Research the content of other labels in the same therapeutic class, including competitor labeling, to help guide the team in developing labeling text, including contingency strategy development for negotiation with regulatory authorities.
  • Responsible for proofreading and departmental QC work; ensure quality of labeling deliverables (e.g., alignment of labeling text with data, regulatory requirements, consistency between labeling documents).
  • Liaise with cross functional members and stakeholders to obtain input pertaining to labeling including resolution of key regulatory issues and labeling changes .
  • Partner with Clinical Regulatory and cross-functional teams to support labeling supplements and updates, and health authority interactions related to labeling
  • Ensure the dissemination of approved labeling documents and supporting documentation.
  • Maintain controlled records for all labeling changes and communicate labeling updates to stakeholders at the time of implementation.
  • Build partnerships with key stakeholders from other functions to ensure that strategic business goals are met through the sharing of knowledge and expertise.
  • Participate in any relevant continuous improvement efforts for the end-to-end labeling process.
  • Monitor global regulatory environment and assess impact of changes on business and product labeling activities.
  • Facilitate policy development and updates with internal stakeholders.

Requirements
  • Bachelor's degree in life sciences, computer science, or related science discipline
  • Minimum 8+ in the biotech or pharmaceutical industry leading the development/maintenance of product labeling across two or more major geographic areas.
  • Knowledge of advertising promotion regulations and FDA Guidance documents issued with some technical experience in aspects of drug development and labeling
  • Experience leading cross-functional meetings and facilitating strategic discussions, such as negotiating with internal stakeholders and regulatory authorities on complex labeling issues.
  • Ability to review regulatory labeling documents for accuracy and adherence to regulatory requirements, noting deviations and inconsistencies.
  • Strong knowledge of document formatting (MS Word documents, PDFs compliance, and validation tools)
  • Ability to maintain highest degree of professionalism, integrity and diplomacy

Preferred
  • Experience with regulatory information management systems (e.g., Veeva RIM, Registrations).
  • Knowledgeable in emerging technologies, including AI applications in regulatory operations.
  • Experience supporting global inspection readiness.

California pay range
$210,000-$230,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
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